NDC 81745-301 Atoa
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 81745-301?
What are the uses for Atoa?
Which are Atoa UNII Codes?
The UNII codes for the active ingredients in this product are:
- RICE BRAN (UNII: R60QEP13IC)
- RICE BRAN (UNII: R60QEP13IC) (Active Moiety)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) (Active Moiety)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (Active Moiety)
- OPUNTIA HUMIFUSA WHOLE (UNII: 6E9O5V4SS5)
- OPUNTIA HUMIFUSA WHOLE (UNII: 6E9O5V4SS5) (Active Moiety)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX) (Active Moiety)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- ASIAN GINSENG (UNII: CUQ3A77YXI) (Active Moiety)
Which are Atoa Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ASTRAGALUS PROPINQUUS ROOT POLYSACCHARIDES (UNII: 71WW2LNL50)
- WATER (UNII: 059QF0KO0R)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- GLYCERYL CAPRATE (UNII: 197M6VFC1W)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- RICE BRAN OIL (UNII: LZO6K1506A)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".